As a family caregiver, you answer questions all day long. Who's her neurologist? What's her blood pressure? When did she eat today? Where is her new walker? Why is she sleeping? Fact based, straightforward and usually easy to answer questions.
The most difficult question is more opinion based, more revealing, more sensitive. For me the question is: How is your Mom? It's also the most personal question because most of my decisions each day revolve around the answer to the question: How is your Mom?
When Mom first became ill in the Fall of 2012, the answer was easy: Mom's a fighter, she's strong and getting better every day! She had a gastro-intestinal issue that required a lengthy surgery right after Hurricane Sandy. In the recovery room she had us laughing because she whispered to us "I guess I won't be able to wear a bikini". My mother doesn't wear a bikini! My mother's sense of humor was alive and well and I knew she would be OK. She bounced back within a few months.
When Mom fell in the Fall of 2014, she broke her arm. She had fallen right before my eyes, like a tree that had been chopped down. We had lots of questions. She was in the hospital for several days and then we had our first experience with rehab. Our choice of rehab was terrible and we brought her home within 5 days. I earned the title of Advocate for my mother and the answer to the question was getting harder. She wasn't as resilient, not fighting as hard to get well. Mom was OK and needed physical therapy to get back on her feet.
This past year was difficult for Mom. She fell and broke her hip in May and then fell and broke ribs in September. Her health is deteriorating. She needs constant care. We are frequent fliers with the Visiting Nurse program and Home Health agencys who all ask, "How is your Mother"?
On good days, the answer is Mom is OK, today was a good day. I usually post silly selfies of Mom and I and try to keep things positive.
On bad days, the answer is Mom is OK. We know that sometimes making it through another day without major incident is all we can do.
No one really wants to hear the ins and outs of caregiving. What foods we experimented with to try to get mom to eat. What music worked today but won't work tomorrow to get her to walk. Or how her hands won't open any more.
The reality is my mother is not going to get better. The Parkinson's Disease is winning, robbing her of the ability to walk, talk and care for herself. My Mother is a fighter, a strong woman but unfortunately she is giving up. I can't say that I blame her. She's been like a Timex watch, she takes a licking and keeps on ticking. Until now.
Caregiving is hard. There are days when I am so angry. I'm angry because my Dad has lost patience with my mom. I'm angry because I lose at least 2 days a week to caring for my mom. I'm angry because it's really hard to focus on life and get things done when all you think about is your mom.
Caregiving is a gift. I have the luxury of being able to spend time with my mom. I get to experience the good days when she decides she wants to talk and asks me questions! It's an honor to help her at this time in her life after all that she has given me.
I understand the question, How's Your Mom? comes from a place of caring and concern for me, my family and for Mom.
I don't want to answer the question with a simple OK, I want to shout that she's AWFUL, that it's NOT FAIR and no one DESERVES this quality of life. But I can't. That wouldn't be fair to the person asking or my mother. I will continue to be her advocate and preserve her dignity. I will share more information with my closest friends and keep up the good fight.
It's difficult when someone you know is caring for a sick friend or relative. Don't be afraid to ask the most difficult question. Be prepared for a canned response. And know that your simply being there and caring is the world's greatest gift to your friend.
If you are a caregiver, what is the most challenging question you are asked? How to you respond when asked about your caree? Please share your comments below. Let's start a conversation and support each other.
Wishing you peace, love and sparks of perseverance, Deb
Mom and I loved to play Santa to children each year. We would always pick at least one name from the Giving Tree at church and sometimes one from the Giving Trees at work. We would plot and plan our shopping trip to figure out which store would make our money go the farthest because we were trying to buy as many items on each child's list.
This year, Mom and I went to the Mall to simply see the decorations and do a little "targeted shopping". The days of going to the Mall for hours and wandering around with Mom are gone. I push her in her wheelchair and we spend no more than an hour. It breaks my heart. My mother taught me how to shop!
On that day in early December, we had wandered around a bit, bought one or two things, looked at the decorations and were leaving when I spied the Salvation Army Giving Tree! I stood there reading every child's wish to my mother and then selected two children to shower with gifts!
As I shopped, my heart was full and broken at the same time. I missed my mom, who would often say "don't worry about the money, let's just get the gifts" when I was figuring out the best price, package, etc. So, I got the gifts. I bought everything on each child's list. (Let's not get crazy, I did establish a budget and maximized it.)
I told Mom and Dad about my shopping spree and how I had a large shopping bag of gifts for each of the children that included toys, clothes and of course Christmas PJ's. And all within budget! We laughed, smiled and felt the spirit of Christmas. That was our early Christmas Gift.
I know today that Mom gifted me her Giving Spirit. We didn't always have a lot growing up, but we always had enough. We always made time or resources available to give back. When we didn't have extra money, we gave our time. And we had extra money, we gave it. The Giving Spirit.
When I brought the bags of gifts back to the Mall for the Giving Tree, I was happy to give and sad that I was dragging the packages in by myself. My partner in crime was not with me. What I later realized was...Mom was with me, not in person, but in the Giving Spirit.
Do you have a favorite holiday memory with your Mom, Dad or caree? Holiday memories are special. I would love to hear your holiday memories. They are the stories that keep traditions alive! Please share the comments below.
Wishing you peace, love and beautiful memories, Deb
Welcome to Tuesdays with Mom. My goal is to share with you the tears, the laughter, the joys and the frustrations of being a part-time caregiver and a full-time advocate for my mother, Barbara. It's the hardest job I've ever had and yet the most rewarding. My hope is that we can start a conversation, learn from and support each other through this shared experience.
Being a caregiver for a family member is a individual journey, but we are not alone. According to a 2015 AARP study, there are approximately 15.7 million family caregivers in the US providing care for a person with Alzheimer's. Overall, there are nearly 40 million family caregivers who provide care to an adult family member.
If I have 40 million caregiving peers, why does it feel so lonely? It's time for me to reach out and share my stories with the intention of providing and receiving support.
My journey begins 5 years ago when my mother's health started to decline. In the Fall of 2012, she had a major diverticulitis attack which involved perforated intestines and a wicked infection. She spent a week in the hospital then came home with a PICC line for daily antibiotics and a drain for, you know, the infection. (Yuck). While we had the support of wonderful Visiting Nurses, Mom was under the care of Dad and me. We used to kid around that we were B and D Nursing (Bruce and Debbie) and we had no idea that we were predicting the future. That Fall, we made it through 2 months of daily antibiotics and care for Mom.
The night before Mom's surgery was difficult. Prepping for intestinal surgery is worse than preparing for a colonoscopy. Lots of laxatives and antibiotics. Mom has a very strong will and she refused to take some of the medicine. I spent hours with her, cajoling her to take the meds with little success. I made frantic calls to the nurses who assured me everything would be ok. At one point, in sheer frustration, I walked out of the house in tears and went to the mall to clear my head. My Dad was the hero that night, he sat with her, got her to take some of the meds and she eventually settled down and was able to sleep.
She had a lengthy intestinal surgery that was successful except for the part that she was under anesthesia for more than 6 hours. We've learned that anesthesia is not a good thing when potential neuro issues are present. Stay tuned for more on that part of the story.
My Dad is a Funeral Director and the nicest guy I know. He retired in 2008 and was asked to come back to work part-time in 2010. This part-time work was good for my Dad because in retirement, he and my Mom didn't have much to do. They worked hard all of their lives and didn't develop many hobbies.
Dad now works Tuesdays and Fridays, and is Mom's full-time caregiver. Over the past 5 years, when Mom was sick and Dad needed to work, I would spend the day with Mom. As her health has declined, we enrolled Mom is a local Adult Day Center (ADC) which was a great experience for her. At this time, she is unable to return to the ADC program and I spend Tuesdays and Fridays with Mom.
Recently, my boyfriend asked where I was going and I replied, "remember it's Tuesday with Mom". He said "that should be the name of your book" and I replied, "No, it should be the name of my new blog!" and this blog was born.
I hope you will join me here and share your experiences, advice, questions, concerns, tears and laughter. My intention is to create a space where we can support each other as caregivers.
Please leave a comment below. Share a thought, a story. Ask a question. Ask for support. You are not alone.
Wishing you peace, love and inspiration, Deb